Patient, caregiver, health professional and researcher views and experiences of participating in research at the end of life: a critical interpretive synthesis of the literature.
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Ethical aspects of registry-based research in the Nordic countriesCommon or multiple futures for end of life care around the world? Ideas from the 'waiting room of history'Health systems guidance appraisal--a critical interpretive synthesisEvaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews.The effect and process evaluations of the national quality improvement programme for palliative care: the study protocol.Is the patient satisfaction questionnaire an acceptable tool for use in a hospice inpatient setting? A pilot study.End-of-life care research with bereaved informal caregivers--analysis of recruitment strategy and participation rate from a multi-centre validation studyFeasibility of Conducting a Palliative Care Randomized Controlled Trial in Children With Advanced Cancer: Assessment of the PediQUEST StudyThe selection and use of outcome measures in palliative and end-of-life care research: the MORECare International Consensus Workshop.'Best practice' in developing and evaluating palliative and end-of-life care services: a meta-synthesis of research methods for the MORECare project.Using social media in supportive and palliative care research.What the eye does not see: a critical interpretive synthesis of European Union policies addressing sexual violence in vulnerable migrants.Pharmacokinetic considerations and recommendations in palliative care, with focus on morphine, midazolam and haloperidol.The person behind the patient: a feasibility study using the Patient Dignity Question for patients with palliative care needs in hospital.Research on psychological and social factors in palliative care: an invited commentary.Dying persons' perspectives on, or experiences of, participating in research: An integrative review.Primary palliative Care in General Practice - study protocol of a three-stage mixed-methods organizational health services research study.How did partners experience cancer patients' participation in a phase I study? An observational study after a patient's death.Patient and public involvement in the design of clinical trials: An overview of systematic reviews.Knowledge synthesisEditorial
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P2860
Patient, caregiver, health professional and researcher views and experiences of participating in research at the end of life: a critical interpretive synthesis of the literature.
description
2012 nî lūn-bûn
@nan
2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2012年の論文
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2012年論文
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2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
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name
Patient, caregiver, health pro ...... e synthesis of the literature.
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Patient, caregiver, health pro ...... e synthesis of the literature.
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Patient, caregiver, health pro ...... e synthesis of the literature.
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Patient, caregiver, health pro ...... e synthesis of the literature.
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Patient, caregiver, health pro ...... e synthesis of the literature.
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Patient, caregiver, health pro ...... e synthesis of the literature.
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Patient, caregiver, health pro ...... ve synthesis of the literature
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Patient, caregiver, health pro ...... ve synthesis of the literature
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Patient, caregiver, health pro ...... e synthesis of the literature.
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Patient, caregiver, health pro ...... e synthesis of the literature.
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Patient, caregiver, health pro ...... e synthesis of the literature.
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P2860
P356
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Patient, caregiver, health pro ...... ve synthesis of the literature
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P2093
Marjolein H Gysels
P2860
P2888
P356
10.1186/1471-2288-12-123
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2012-08-17T00:00:00Z
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P6179
1007144982